The effect of nocturnal wear of complete dentures on sleep and oral health related quality of life: study protocol for a randomized controlled trial
Identifieur interne : 001658 ( Main/Exploration ); précédent : 001657; suivant : 001659The effect of nocturnal wear of complete dentures on sleep and oral health related quality of life: study protocol for a randomized controlled trial
Auteurs : Elham Emami [Canada] ; Phan The Huy Nguyen ; Fernanda R. Almeida ; Jocelyne S. Feine [Canada] ; Igor Karp ; Gilles Lavigne ; Nelly HuynhSource :
- Trials [ 1745-6215 ] ; 2014.
Descripteurs français
- KwdFr :
- Enquêtes et questionnaires, Facteurs temps, Femelle, Humains, Indice de gravité médicale, Mâchoire édentée (), Mâchoire édentée (psychologie), Mâchoire édentée (rééducation et réadaptation), Mâle, Méthode en simple aveugle, Plan de recherche, Prothèse dentaire complète (effets indésirables), Protocoles cliniques, Qualité de vie, Québec, Santé buccodentaire, Sommeil, Sujet âgé, Syndrome d'apnées obstructives du sommeil (), Syndrome d'apnées obstructives du sommeil (diagnostic), Syndrome d'apnées obstructives du sommeil (physiopathologie), Syndrome d'apnées obstructives du sommeil (étiologie), Études croisées.
- MESH :
- diagnostic : Syndrome d'apnées obstructives du sommeil.
- effets indésirables : Prothèse dentaire complète.
- physiopathologie : Syndrome d'apnées obstructives du sommeil.
- psychologie : Mâchoire édentée.
- rééducation et réadaptation : Mâchoire édentée.
- étiologie : Syndrome d'apnées obstructives du sommeil.
- Enquêtes et questionnaires, Facteurs temps, Femelle, Humains, Indice de gravité médicale, Mâchoire édentée, Mâle, Méthode en simple aveugle, Plan de recherche, Protocoles cliniques, Qualité de vie, Québec, Santé buccodentaire, Sommeil, Sujet âgé, Syndrome d'apnées obstructives du sommeil, Études croisées.
English descriptors
- KwdEn :
- Aged, Clinical Protocols, Cross-Over Studies, Denture, Complete (adverse effects), Female, Humans, Jaw, Edentulous (complications), Jaw, Edentulous (psychology), Jaw, Edentulous (rehabilitation), Male, Oral Health, Quality of Life, Quebec, Research Design, Severity of Illness Index, Single-Blind Method, Sleep, Sleep Apnea, Obstructive (diagnosis), Sleep Apnea, Obstructive (etiology), Sleep Apnea, Obstructive (physiopathology), Sleep Apnea, Obstructive (prevention & control), Surveys and Questionnaires, Time Factors.
- MESH :
- geographic : Quebec.
- adverse effects : Denture, Complete.
- complications : Jaw, Edentulous.
- diagnosis : Sleep Apnea, Obstructive.
- etiology : Sleep Apnea, Obstructive.
- physiopathology : Sleep Apnea, Obstructive.
- prevention & control : Sleep Apnea, Obstructive.
- psychology : Jaw, Edentulous.
- rehabilitation : Jaw, Edentulous.
- Aged, Clinical Protocols, Cross-Over Studies, Female, Humans, Male, Oral Health, Quality of Life, Research Design, Severity of Illness Index, Single-Blind Method, Sleep, Surveys and Questionnaires, Time Factors.
Abstract
Edentulism and sleep disturbance are chronic conditions that are common in older people and have serious adverse consequences for their functioning and quality of life. Edentulism can disturb sleep through the alteration of the craniofacial structure and surrounding soft tissue. However, the effect of prosthetic rehabilitation of edentulism on sleep quality is still not well understood. The objectives of this study are to test whether nocturnal denture wear affects sleep quality, daytime sleepiness, and the oral health related quality of life of edentate older people with moderate to severe sleep apnea, and to identify modifiers of effect of nocturnal denture wear.
We will carry out a single-blind randomized cross-over trial. Seventy edentate older people with moderate to severe obstructive sleep apnea will be enrolled. The study participants will be assigned to wear and not wear their dentures on alternate periods of 30 days. The outcome measures will be sleep quality (assessed by portable polysomnography), daytime sleepiness (assessed by the Epworth Sleepiness Scale), and oral health related quality of life (assessed by validated questionnaire). A number of characteristics (sociodemographic, oropharyngeal morphology, oral and prosthesis characteristics, and perceived general health quality of life) will be assessed by means of clinical examination, 3D imaging of the craniofacial structure, and validated questionnaires at baseline. Linear mixed effects regression models for repeated measures will be fitted to test the study hypotheses. The main analyses will be based on the intention-to-treat principle. To assess the robustness of the findings to potential incomplete adherence, sensitivity analyses will be conducted while applying the per-protocol principle.
This practice-relevant evidence could represent a preventive approach to improve sleep characteristics of the older population and improve their well-being and quality of life.
ClinicalTrials.gov
Url:
DOI: 10.1186/1745-6215-15-358
PubMed: 25218696
PubMed Central: 4177759
Affiliations:
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Le document en format XML
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<term>Clinical Protocols</term>
<term>Cross-Over Studies</term>
<term>Denture, Complete (adverse effects)</term>
<term>Female</term>
<term>Humans</term>
<term>Jaw, Edentulous (complications)</term>
<term>Jaw, Edentulous (psychology)</term>
<term>Jaw, Edentulous (rehabilitation)</term>
<term>Male</term>
<term>Oral Health</term>
<term>Quality of Life</term>
<term>Quebec</term>
<term>Research Design</term>
<term>Severity of Illness Index</term>
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<term>Sleep Apnea, Obstructive (diagnosis)</term>
<term>Sleep Apnea, Obstructive (etiology)</term>
<term>Sleep Apnea, Obstructive (physiopathology)</term>
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<term>Surveys and Questionnaires</term>
<term>Time Factors</term>
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<keywords scheme="KwdFr" xml:lang="fr"><term>Enquêtes et questionnaires</term>
<term>Facteurs temps</term>
<term>Femelle</term>
<term>Humains</term>
<term>Indice de gravité médicale</term>
<term>Mâchoire édentée ()</term>
<term>Mâchoire édentée (psychologie)</term>
<term>Mâchoire édentée (rééducation et réadaptation)</term>
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<term>Méthode en simple aveugle</term>
<term>Plan de recherche</term>
<term>Prothèse dentaire complète (effets indésirables)</term>
<term>Protocoles cliniques</term>
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<term>Santé buccodentaire</term>
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<term>Sujet âgé</term>
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<term>Syndrome d'apnées obstructives du sommeil (diagnostic)</term>
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<term>Syndrome d'apnées obstructives du sommeil (étiologie)</term>
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<term>Humains</term>
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<front><div type="abstract" xml:lang="en"><sec><title>Background</title>
<p>Edentulism and sleep disturbance are chronic conditions that are common in older people and have serious adverse consequences for their functioning and quality of life. Edentulism can disturb sleep through the alteration of the craniofacial structure and surrounding soft tissue. However, the effect of prosthetic rehabilitation of edentulism on sleep quality is still not well understood. The objectives of this study are to test whether nocturnal denture wear affects sleep quality, daytime sleepiness, and the oral health related quality of life of edentate older people with moderate to severe sleep apnea, and to identify modifiers of effect of nocturnal denture wear.</p>
</sec>
<sec><title>Methods/design</title>
<p>We will carry out a single-blind randomized cross-over trial. Seventy edentate older people with moderate to severe obstructive sleep apnea will be enrolled. The study participants will be assigned to wear and not wear their dentures on alternate periods of 30 days. The outcome measures will be sleep quality (assessed by portable polysomnography), daytime sleepiness (assessed by the Epworth Sleepiness Scale), and oral health related quality of life (assessed by validated questionnaire). A number of characteristics (sociodemographic, oropharyngeal morphology, oral and prosthesis characteristics, and perceived general health quality of life) will be assessed by means of clinical examination, 3D imaging of the craniofacial structure, and validated questionnaires at baseline. Linear mixed effects regression models for repeated measures will be fitted to test the study hypotheses. The main analyses will be based on the intention-to-treat principle. To assess the robustness of the findings to potential incomplete adherence, sensitivity analyses will be conducted while applying the per-protocol principle.</p>
</sec>
<sec><title>Discussion</title>
<p>This practice-relevant evidence could represent a preventive approach to improve sleep characteristics of the older population and improve their well-being and quality of life.</p>
</sec>
<sec><title>Trial registration</title>
<p>ClinicalTrials.gov <ext-link ext-link-type="uri" xlink:href="http://www.clinicaltrials.gov/NCT01868295">NCT01868295</ext-link>
.</p>
</sec>
</div>
</front>
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<affiliations><list><country><li>Canada</li>
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<settlement><li>Montréal</li>
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